Sur les moments atomiques et les points de Curie dans les solutions solides du nickel

Marian, V G

doi:10.1051/jphysrad:0193700807031300

Cited by 3 publications

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“…It was soon realized [6] that if the kinetics of growth and solute depletion could be measured independently the rate constants k and j could also be determined independently, enabling r to be estimated without the need to know the value ofD and vice versa. Borrowing from original ideas of Ben Israel and Fine [7], and taking advantage of the very strong dependence on Al content of the ferromagnetic Curie temperature of Ni [8], the kinetics of solute depletion in Ni-Al alloys [9] were measured and the equation…”

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A1-L12 interfacial free energies from data on coarsening in five binary Ni alloys, informed by thermodynamic phase diagram assessments

Ardell

2011

J Mater Sci

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The data on coarsening of c 0 -type precipitates (Ni 3 X, with the L1 2 crystal structure) in Ni-Al, Ni-Ga, Ni-Ge, Ni-Si, and Ni-Ti alloys are re-evaluated in the context of recent (TIDC) and classical (LSW) theories of coarsening, with the objective of ascertaining the best values possible of interfacial free energies, r, of the c/c 0 interfaces in these five alloy systems. The re-evaluations include fitting of the particle size distributions, reanalyzing all the available data on the kinetics of particle growth and kinetics of solute depletion, and using thermodynamic assessments of the binary alloy phase diagrams to calculate curvatures of the Gibbs free energies of mixing. The product of the work is two sets of interfacial free energies, one set for the analysis using the recent TIDC theory and the other for the analysis using the classical LSW theory. The TIDC-based analysis yields lower values of r by about a factor of 2/3. All the interfacial energies are considerably larger, by factors ranging from *4 to 10, than those previously reported, which were for the most part calculated from data on coarsening assuming idealsolution thermodynamics. In the TIDC theory the width of the interface, d, is allowed to increase with particle size, r. A simple equation relating r to the ratio of the gradient energy and d is used to show that r can remain constant even though d increases with r. Published work supporting this contention is presented and discussed.

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